255324009: Movement (observable entity)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

380509014 Movement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

380510016 Quality of movement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2528848014 Movement (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

42051000077112 mouvement fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
mouvement	Is a	Gross motor functions (observable entity)	false	Inferred relationship	Some
mouvement	Is a	Process (observable entity)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Amyotrophic lateral sclerosis with parkinsonism	Interprets	False	mouvement	Inferred relationship	Some	3
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Dissociative neurological symptom disorder with tremor (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder)	Interprets	False	mouvement	Inferred relationship	Some	5
Ataxia due to subpial siderosis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Ataxia due to acquired vitamin deficiency	Interprets	False	mouvement	Inferred relationship	Some	2
Autoimmune movement disorder	Interprets	False	mouvement	Inferred relationship	Some	1
Adult-onset tic disorder (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Adult-onset sporadic primary dystonia	Interprets	False	mouvement	Inferred relationship	Some	3
Adult-onset familial idiopathic dystonia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Autosomal dominant complex hereditary spastic paraplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	6
Chorea due to neuroferritinopathy	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to mitochondrial cytopathy	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to classical pantothenate kinase associated neurodegeneration (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to polycythemia rubra vera	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to Lesch-Nyhan syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to paraneoplastic syndrome	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to Huntington disease-like 3 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to Huntington disease-like 2 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to hyperglycemia	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to hereditary ataxia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to antiphospholipid syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to ataxia telangiectasia syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to endocrine disorder	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to chronic hepatocerebral degeneration	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to anoxia of brain (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to Huntington disease-like 1 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to and following ventriculoperitoneal shunt (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Chorea due to inherited aminoaciduria (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to prion disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to tardive dyskinesia	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to cerebral injury due to birth trauma (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to inherited organic acidemia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to hyponatremia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to hypoparathyroidism (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to widespread metastatic malignant neoplastic disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to and following injury of head (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to immunological disorder (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to inborn error of metabolism (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea due to metabolic disorder	Interprets	False	mouvement	Inferred relationship	Some	1
Chorea caused by dopamine receptor antagonist (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Congenital multi-minicore disease with external ophthalmoplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea caused by oral contraceptive (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
A rare genetic syndromic intellectual disability characterised by global developmental delay, moderate to severe intellectual disability, motor and language impairment, behavioural abnormalities (with mood instability, aggression, and self-mutilation), and progressive hand tremor. Facial dysmorphism includes narrow palpebral fissures, large ears, long philtrum, and prominent chin.	Interprets	False	mouvement	Inferred relationship	Some	5
A rare genetic neurological disorder characterized by the association of congenital spastic paraplegia with global developmental delay and intellectual disability, ophthalmologic abnormalities (including nystagmus, reduced visual acuity, or hypermetropia), and obesity. Additional manifestations are brachy plagiocephaly and dysmorphic facial features. Brain imaging may show dilated ventricles, abnormal myelination, and mild generalized atrophy. Homozygous loss-of-function variants of KIDINS220 associated with a fetal lethal phenotype with ventriculomegaly and limb contractures have been reported.	Interprets	False	mouvement	Inferred relationship	Some	10
Hemichorea due to injury of head (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Hemichorea due to cerebral arteriovenous malformation (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Hemichorea due to abscess of brain (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to Lesch Nyhan syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Hemichorea due to cerebral hemorrhage (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to glutaric acidemia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to GM2 gangliosidosis	Interprets	False	mouvement	Inferred relationship	Some	3
Parkinsonism caused by dopamine receptor antagonist (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Parkinsonism caused by dopamine depleting agent (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to hereditary disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to homocystinuria (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to hereditary spastic paraplegia (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to head injury (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to neutral 1 amino acid transport defect (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to metachromatic leucodystrophy (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Hemichorea due to neoplasm of brain (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Hemichorea due to cerebral infarction (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Hemichorea due to multiple sclerosis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to Pelizaeus-Merzbacher disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to mitochondrial disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to Niemann-Pick disease type C (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to Rett syndrome	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to perinatal cerebral injury (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to encephalitis	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to disorder of peripheral nervous system (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to cerebral anoxia	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to ataxia telangiectasia syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia caused by dopamine receptor antagonist (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Dystonia due to focal brain lesion	Interprets	False	mouvement	Inferred relationship	Some	3
Dystonia due to familial basal ganglia calcifications	Interprets	False	mouvement	Inferred relationship	Some	2
Jumpy stump syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	1
Dystonia due to Wilson disease (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Myoclonic disorder due to dementia	Interprets	False	mouvement	Inferred relationship	Some	3
Myoclonic disorder due to sialidosis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Myoclonic disorder due to mitochondrial disorder (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Myoclonic disorder due to hepatic failure (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Myoclonic disorder due to neuronal ceroid lipofuscinosis (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Myoclonic disorder due to uremia	Interprets	False	mouvement	Inferred relationship	Some	2
Familial multiple system tauopathy	Interprets	False	mouvement	Inferred relationship	Some	2
Chorea gravidarum	Interprets	False	mouvement	Inferred relationship	Some	3
Fahr's syndrome (disorder)	Interprets	False	mouvement	Inferred relationship	Some	3
Westphal-Strumpell syndrome	Interprets	False	mouvement	Inferred relationship	Some	4
Drug-induced chorea	Interprets	False	mouvement	Inferred relationship	Some	3
Basal ganglia degeneration with calcification	Interprets	False	mouvement	Inferred relationship	Some	2
Aicardi Goutieres syndrome	Interprets	False	mouvement	Inferred relationship	Some	2
Autosomal dominant late onset basal ganglia degeneration	Interprets	False	mouvement	Inferred relationship	Some	2
Aicardi Goutieres syndrome type 1	Interprets	False	mouvement	Inferred relationship	Some	2
Aicardi Goutieres syndrome type 2	Interprets	False	mouvement	Inferred relationship	Some	2
Aicardi Goutieres syndrome type 3	Interprets	False	mouvement	Inferred relationship	Some	2
Aicardi Goutieres syndrome type 4 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Aicardi Goutieres syndrome type 5 (disorder)	Interprets	False	mouvement	Inferred relationship	Some	2
Oral choreiform movement	Interprets	False	mouvement	Inferred relationship	Some	4
Chorea co-occurrent and due to Huntington disease-like condition (disorder)	Interprets	False	mouvement	Inferred relationship	Some	4
Paroxysmal choreoathetosis	Interprets	False	mouvement	Inferred relationship	Some	4
Choreoathetosis	Interprets	False	mouvement	Inferred relationship	Some	3

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Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
380509014	Movement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
380510016	Quality of movement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2528848014	Movement (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
42051000077112	mouvement	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module